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The proposed long‐term management plan for used nuclear fuel is to isolate it within a multiple‐barrier system underground in a deep geological repository (DGR). In the Canadian design, used fuel bundles will be sealed in copper‐coated carbon steel used fuel containers, encased in blocks of bentonite clay, emplaced approximately 500–800 m below ground, and surrounded by a bentonite gapfill material. A laboratory experimental campaign has been undertaken to demonstrate the integrity of the multiple‐barrier system. DGR‐relevant copper materials were embedded in bentonite clay, compacted to various densities, and sealed into a hermetic pressure vessel pressurized with demineralized water. Experiments explored the influence of bentonite compaction in the range of 1100–1600 kg/m3 on copper corrosion over durations of 1–18 months. Postexposure analysis of the copper coupons showed nonhomogeneous corrosion, with corrosion products composed of Cu2O, with some Cu2S. The average corrosion rates decreased as a function of time and increasing bentonite compaction density. In general, we observed that higher bentonite compaction density suppressed the corrosion of embedded copper. [ABSTRACT FROM AUTHOR]

The strategy for the permanent disposal of high‐level nuclear waste in Canada involves sealing it in a copper‐coated steel container and burying it in a deep geologic repository. During the early emplacement period, the container could be exposed to warm humid air, which could result in the condensation of nitric acid, produced by the radiolysis of the humid air, on the copper surface. Previous studies have suggested that both nitrate and oxygen reduction will drive copper corrosion, with the nitrate reduction kinetics being dependent on the concentration of soluble copper(I) produced by the anodic dissolution of copper in the reaction with oxygen. This study focused on determining the kinetics of nitrate and oxygen reduction and elucidating the synergistic relationship between the two processes. This was investigated using corrosion potential and polarization measurements in conjunction with scanning electron microscopy and X‐ray photoelectron spectroscopy. Oxygen reduction was shown to be the dominant cathodic reaction with the oxidation of copper(I) to copper(II) by nitrate, promoting the catalytic cycle involving the reaction of copper(II) with copper to reproduce copper(I). [ABSTRACT FROM AUTHOR]